FMR1, FMRP translational regulator 1, 2332

N. diseases: 346; N. variants: 10
Disease: Dyssomnias ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0700201
Disease: Dyssomnias
Dyssomnias 		0.010 GeneticVariation disease BEFREE Individuals with autism spectrum disorders (ASD) who have an identifiable single-gene neurodevelopmental disorder (NDD), such as fragile X syndrome (FXS, FMR1), Smith-Magenis syndrome (SMS, RAI1), or 2q23.1 deletion syndrome (del 2q23.1, MBD5) share phenotypic features, including a high prevalence of sleep disturbance. 25271084 2015